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RU2416603C2 - Aminodihydrothiazine derivatives - Google Patents

Aminodihydrothiazine derivatives Download PDF

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Publication number
RU2416603C2
RU2416603C2 RU2008120601A RU2008120601A RU2416603C2 RU 2416603 C2 RU2416603 C2 RU 2416603C2 RU 2008120601 A RU2008120601 A RU 2008120601A RU 2008120601 A RU2008120601 A RU 2008120601A RU 2416603 C2 RU2416603 C2 RU 2416603C2
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RU
Russia
Prior art keywords
optionally substituted
hydrogen atom
pharmaceutically acceptable
solvate
acceptable salt
Prior art date
Application number
RU2008120601A
Other languages
Russian (ru)
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RU2008120601A (en
RU2416603C9 (en
Inventor
Наотаке КОБАЯСИ (JP)
Наотаке КОБАЯСИ
Казуо УЕДА (JP)
Казуо УЕДА
Наохиро ИТОХ (JP)
Наохиро ИТОХ
Синдзи СУЗУКИ (JP)
Синдзи СУЗУКИ
Гаку САКАГУТИ (JP)
Гаку САКАГУТИ
Акира КАТО (JP)
Акира КАТО
Акира ЮКИМАСА (JP)
Акира ЮКИМАСА
Акихиро ХОРИ (JP)
Акихиро Хори
Юдзи КОРИЯМА (JP)
Юдзи КОРИЯМА
Хидеказу ХАРАГУТИ (JP)
Хидеказу ХАРАГУТИ
Кен ЯСУИ (JP)
Кен ЯСУИ
Ясухико КАНДА (JP)
Ясухико КАНДА
Original Assignee
Сионоги Энд Ко., Лтд.
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Publication of RU2008120601A publication Critical patent/RU2008120601A/en
Publication of RU2416603C2 publication Critical patent/RU2416603C2/en
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Publication of RU2416603C9 publication Critical patent/RU2416603C9/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425—Thiazoles
    • A61K31/426—1,3-Thiazoles
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
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    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
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    • C07D265/06—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings
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    • C07D471/04—Ortho-condensed systems

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Abstract

FIELD: chemistry.
SUBSTANCE: described is a composition with inhibitory activity on BACE1, which contains a compound of general formula
Figure 00000380
(I), where ring A is an optionally substituted carbocyclic group or an optionally substituted heterocyclic group; E denotes a lower alkylene; X is S, O or NR1; R1 denotes a hydrogen atom or lower alkyl; each R2a, R2b, R3a, R3b, R4a and R4b independently denotes a hydrogen atom, an optionally substituted alkyl or optionally substituted carbocyclic group; each n and m independently denotes an integer from 0 and 3; n+m equals an integer from 1 to 3; R5 denotes a hydrogen atom or an optionally substituted lower alkyl; a pharmaceutically acceptable salt or solvate thereof. Described also is a compound of formula (I) and a pharmaceutical composition.
EFFECT: highly effective treatment.
21 cl, 170 tbl, 4 ex

Description

Текст описания приведен в факсимильном виде.

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Claims (21)

1. Композиция с ингибиторной активностью в отношении ВАСЕ 1, содержащая терапевтически эффективное количество соединения, представленного общей формулой (I):
химическая формула 1
Figure 00000345

где цикл А представляет собой необязательно замещенную карбоциклическую группу, выбранную из арила и неароматической сопряженной карбоциклической группы или необязательно замещенную гетероциклическую группу, выбраную из гетероциклической группы, содержащей один или несколько гетероатомов, выбранных из О, S и N;
химическая формула 2
Figure 00000346
обозначает
Figure 00000347
,
Figure 00000348

Alk1 обозначает низший алкилен или низший алкенилен;
Х обозначает S, О или NR1;
R1 обозначает атом водорода или низший алкил;
каждый из R2a и R2b независимо обозначает атом водорода, необязательно замещенный низший алкил, необязательно замещенный амидино, необязательно замещенный ацил, необязательно замещенный низший алкилсульфонил;
каждый из R3a, R3b, R4a и R4b независимо обозначает атом водорода, необязательно замещенный низший алкил, необязательно замещенную карбоциклическую группу;
каждый из n и m независимо обозначает целое число от 0 до 3;
n+m равно целому числу от 1 до 3;
независимо друг от друга все заместители R3a, R3b, R4a и R4b могут иметь разные значения;
R5 обозначает атом водорода, необязательно замещенный низший алкил, необязательно замещенную карбоциклическую группу;
химическая формула 3
если
Figure 00000346
обозначает
Figure 00000347

R5 и цикл А могут быть взяты вместе с образованием
Figure 00000349

где каждый из R5a и R5b независимо обозначает атом водорода или низший алкил,
s обозначает целое число от 1 до 4;
каждый R5a и каждый R5b могут иметь разные значения;
за исключением соединения, в котором n+m равно 2; R5 обозначает атом водорода; а цикл А представляет собой незамещенный фенил,
его фармацевтически приемлемую соль или сольват, и фармацевтически приемлемый носитель.1. A composition with inhibitory activity against BACE 1, containing a therapeutically effective amount of a compound represented by general formula (I):
chemical formula 1
Figure 00000345

where cycle A represents an optionally substituted carbocyclic group selected from aryl and a non-aromatic conjugated carbocyclic group or an optionally substituted heterocyclic group selected from a heterocyclic group containing one or more heteroatoms selected from O, S and N;
chemical formula 2
Figure 00000346
denotes
Figure 00000347
,
Figure 00000348

Alk 1 is lower alkylene or lower alkenylene;
X is S, O or NR 1 ;
R 1 represents a hydrogen atom or lower alkyl;
each of R 2a and R 2b independently represents a hydrogen atom, optionally substituted lower alkyl, optionally substituted amidino, optionally substituted acyl, optionally substituted lower alkylsulfonyl;
each of R 3a , R 3b , R 4a and R 4b independently represents a hydrogen atom, an optionally substituted lower alkyl, an optionally substituted carbocyclic group;
each of n and m independently represents an integer from 0 to 3;
n + m is an integer from 1 to 3;
independently of each other, all substituents R 3a , R 3b , R 4a and R 4b may have different meanings;
R 5 represents a hydrogen atom, an optionally substituted lower alkyl, an optionally substituted carbocyclic group;
chemical formula 3
if
Figure 00000346
denotes
Figure 00000347

R 5 and cycle A can be taken together to form
Figure 00000349

where each of R 5a and R 5b independently represents a hydrogen atom or lower alkyl,
s is an integer from 1 to 4;
each R 5a and each R 5b may have different meanings;
with the exception of a compound in which n + m is 2; R 5 represents a hydrogen atom; and cycle A is unsubstituted phenyl,
a pharmaceutically acceptable salt or solvate thereof; and a pharmaceutically acceptable carrier. 2. Композиция с ингибиторной активностью в отношении ВАСЕ 1 по п.1, где Х обозначает S.2. A composition with inhibitory activity against BACE 1 according to claim 1, where X is S. 3. Композиция с ингибиторной активностью в отношении ВАСЕ 1 по п.1, где n равно 2, a m равно 0.3. The composition with inhibitory activity against BACE 1 according to claim 1, where n is 2, a m is 0. 4. Композиция с ингибиторной активностью в отношении ВАСЕ 1 по п.1, где Е обозначает связь.4. A composition with inhibitory activity against BACE 1 according to claim 1, where E is a bond. 5. Соединение общей формулы (I):
химическая формула 4
Figure 00000345

где все символы имеют значения, указанные в п.1, при условии, что нижеследующие соединения исключаются:
(i) где R5 представляет собой атом водорода и цикл А представляет собой незамещенный фенил;
(ii) где n равно 1 или 2, m равно 0, R2a обозначает атом водорода, R2b обозначает атом водорода или ацетил, R5 обозначает метил, и цикл А обозначает фенил или 4-метоксифенил;
(iii) где n равно 2, m равно 0, R2a обозначает атом водорода, R2b обозначает атом водорода или ацетил, R5 обозначает этил, и цикл А обозначает 3,4-диметоксифенил;
(iv) где n равно 2, m равно 0, R2a обозначает атом водорода, R2b обозначает атом водорода или ацетил, R5 и кольцо А обозначают фенил;
(v) где n равно 2, m равно 0, R2a и R2b обозначают атом водорода, R5 и кольцо А, взятые вместе, образуют
химическая формула 5
Figure 00000350

где Me обозначает метил, а каждый из символов имеет значения, указанные выше;
(vi) где m+n равно 2, R5 обозначает атом водорода, цикл А представляет собой фенил, замещенный одним или двумя заместителями, выбранными из группы, состоящей из гидрокси, галогена, низшего алкила, низшего алкокси, нитро, амино, низшего алкилкарбониламино, меркапто, низшего алкилтио, и карбамоил,
незамещенный фенил, или
незамещенный нафтил;
(vii) где n равно 1, m равно 0, Х обозначает S, R2a и R2b обозначают атом водорода, R5 обозначает атом водорода, Е обозначает метилен или этилен и цикл А обозначает (а) пиридин, необязательно замещенный одним или двумя заместителями, выбранными из группы, состоящей из гидрокси, алкила, галогена и алкокси, (b) тиофен (с) пиримидин, (d) тиазол, (е) морфолин, (f) тиоморфолин, необязательно замещенный оксо, (g) пиперидин, необязательно замещенный фенилом, или (h) пиперазин, необязательно замещенный одним или двумя заместителями, выбранными из группы, состоящей из алкила, бензила, фенила, пиридила и пиримидила; и
(viii) где n+m равно 1, Х обозначает О, цикл А обозначает (а) фенил, необязательно замещенный галогеном или галогенметилом, или (b) оксазол, замещенный метилом и алкиламино;
его фармацевтически приемлемая соль, или сольват его.5. The compound of General formula (I):
chemical formula 4
Figure 00000345

where all symbols have the meanings specified in paragraph 1, provided that the following compounds are excluded:
(i) where R 5 represents a hydrogen atom and cycle A represents unsubstituted phenyl;
(ii) where n is 1 or 2, m is 0, R 2a is a hydrogen atom, R 2b is a hydrogen atom or acetyl, R 5 is methyl, and cycle A is phenyl or 4-methoxyphenyl;
(iii) where n is 2, m is 0, R 2a is a hydrogen atom, R2b is a hydrogen atom or acetyl, R 5 is ethyl, and cycle A is 3,4-dimethoxyphenyl;
(iv) where n is 2, m is 0, R 2a is a hydrogen atom, R 2b is a hydrogen atom or acetyl, R 5 and ring A are phenyl;
(v) where n is 2, m is 0, R 2a and R 2b represent a hydrogen atom, R 5 and ring A, taken together, form
chemical formula 5
Figure 00000350

where Me is methyl, and each of the symbols has the meanings indicated above;
(vi) where m + n is 2, R 5 is a hydrogen atom, cycle A is phenyl substituted with one or two substituents selected from the group consisting of hydroxy, halogen, lower alkyl, lower alkoxy, nitro, amino, lower alkylcarbonylamino , mercapto, lower alkylthio, and carbamoyl,
unsubstituted phenyl, or
unsubstituted naphthyl;
(vii) where n is 1, m is 0, X is S, R 2a and R 2b are a hydrogen atom, R 5 is a hydrogen atom, E is methylene or ethylene, and cycle A is (a) pyridine optionally substituted with one or two substituents selected from the group consisting of hydroxy, alkyl, halogen and alkoxy, (b) thiophene (c) pyrimidine, (d) thiazole, (e) morpholine, (f) thiomorpholine, optionally substituted oxo, (g) piperidine, optional substituted with phenyl, or (h) piperazine optionally substituted with one or two substituents selected from the group consisting of al yl, benzyl, phenyl, pyridyl and pyrimidyl; and
(viii) where n + m is 1, X is O, cycle A is (a) phenyl optionally substituted with halogen or halogenmethyl, or (b) oxazole substituted with methyl and alkylamino;
a pharmaceutically acceptable salt thereof, or a solvate thereof. 6. Соединение по п.5, где Х обозначает S, его фармацевтически приемлемая соль или сольват.6. The compound of claim 5, wherein X is S, a pharmaceutically acceptable salt or solvate thereof. 7. Соединение по п.6, где n равно 2, a m равно 0, его фармацевтически приемлемая соль или сольват.7. The compound according to claim 6, where n is 2, a m is 0, its pharmaceutically acceptable salt or solvate. 8. Соединение по любому из пп.5-7, где R5 обозначает необязательно замещенный низший алкил, необязательно замещенную карбоциклическую группу, его фармацевтически приемлемая соль или сольват.8. The compound according to any one of claims 5 to 7, wherein R 5 is an optionally substituted lower alkyl, an optionally substituted carbocyclic group, a pharmaceutically acceptable salt or solvate thereof. 9. Соединение по любому из пп.5-7, где R2a обозначает атом водорода, R2b обозначает атом водорода, необязательно замещенный низший алкил, необязательно замещенный ацил или необязательно замещенный низший алкилсульфонил,
его фармацевтически приемлемая соль или сольват.9. The compound according to any one of claims 5 to 7, wherein R 2a is a hydrogen atom, R 2b is a hydrogen atom, optionally substituted lower alkyl, optionally substituted acyl or optionally substituted lower alkylsulfonyl,
a pharmaceutically acceptable salt or solvate thereof. 10. Соединение по любому из пп.5-7, где NR2aR2b имеет формулу:
химическая формула 6
Figure 00000351
,
Figure 00000352
,
Figure 00000353
,
Figure 00000354

каждый из R6, R7 и R8 независимо обозначает атом водорода или низший алкил;
Y обозначает необязательно замещенный низший алкилен;
Z обозначает О;
его фармацевтически приемлемая соль или сольват.10. The compound according to any one of claims 5 to 7, where NR 2a R 2b has the formula:
chemical formula 6
Figure 00000351
,
Figure 00000352
,
Figure 00000353
,
Figure 00000354

each of R 6 , R 7 and R 8 independently represents a hydrogen atom or lower alkyl;
Y is optionally substituted lower alkylene;
Z is O;
a pharmaceutically acceptable salt or solvate thereof. 11. Соединение по любому из пп.5-7, где цикл А представляет собой необязательно замещенный фенил, его фармацевтически приемлемая соль или сольват.11. The compound according to any one of claims 5 to 7, wherein cycle A is optionally substituted phenyl, a pharmaceutically acceptable salt or solvate thereof. 12. Соединение по любому из пп.5-7, где цикл А имеет формулу
химическая формула
Figure 00000355
или
Figure 00000356

где R9, R10 и R11 обозначают атом водорода или G;
G обозначает галоген, гидрокси, циано, необязательно замещенный низший алкил, необязательно замещенный низший алкокси, необязательно замещенный низший алкенил, необязательно замещенный низший алкинил, карбокси, необязательно замещенный низший алкоксикарбонил, необязательно замещенный амино, необязательно замещенный карбамоил, необязательно замещенный низший алкилсульфонил, необязательно замещенную карбоциклическую группу, необязательно замещенную карбоциклическую оксигруппу, или необязательно замещенную гетероциклическую группу;
каждый заместитель G может независимо отличаться от других;
его фармацевтически приемлемая соль или сольват.12. The compound according to any one of paragraphs.5-7, where cycle a has the formula
chemical formula
Figure 00000355
or
Figure 00000356

where R 9 , R 10 and R 11 represent a hydrogen atom or G;
G is halogen, hydroxy, cyano, optionally substituted lower alkyl, optionally substituted lower alkoxy, optionally substituted lower alkenyl, optionally substituted lower alkynyl, carboxy, optionally substituted lower alkoxycarbonyl, optionally substituted amino, optionally substituted lower alkylsulfonyl, optionally substituted lower alkylsulfonyl a carbocyclic group, an optionally substituted carbocyclic oxy group, or an optionally substituted heterocyclic group y;
each substituent G may be independently different from the others;
a pharmaceutically acceptable salt or solvate thereof. 13. Соединение по любому из пп.5-7, где цикл А имеет формулу
химическая формула 8
Figure 00000355
или
Figure 00000356

где R9, R10 и R11 обозначают атом водорода галоген, гидрокси, циано, необязательно замещенный низший алкил, необязательно замещенный низший алкокси, необязательно замещенный низший алкенил, необязательно замещенный низший алкинил, карбокси, необязательно замещенный низший алкоксикарбонил, необязательно замещенный амино, необязательно замещенный карбамоил, необязательно замещенный низший алкилсульфонил, необязательно замещенную карбоциклическую группу, или необязательно замещенную гетероциклическую оксигруппу; и
G представляют собой соединение формулы:
химическая формула 9
Figure 00000357
,
Figure 00000358
,
Figure 00000359
,
Figure 00000360
,
Figure 00000361
,
Figure 00000362
,
Figure 00000363
,
Figure 00000364
,
Figure 00000365
,
Figure 00000366
,
Figure 00000367
,
Figure 00000368
,
Figure 00000369
,
Figure 00000370
,
Figure 00000371

Figure 00000372
,
Figure 00000373
или
Figure 00000374

каждый из Q1, Q2 и Q3 независимо обозначает связь, необязательно замещенный низший алкилен или необязательно замещенный низший алкенилен;
Q4 обозначает необязательно замещенный низший алкилен или необязательно замещенный низший алкенилен;
каждый из W1 и W2 независимо обозначает О или S;
W3 обозначает О, S или NR12;
R12 обозначает атом водорода, низший алкил, гидрокси низший алкил, низший алкокси низший алкил, низший алкоксикарбонил низший алкил;
R14 обозначает атом водорода или низший алкил;
цикл В представляет собой необязательно замещенную карбоциклическую группу, где карбоциклическая группа необязательно выбрана из арила и неароматической конденсированной карбоциклической группы, или необязательно замещенную гетероциклическую группу, где гетероциклическая группа выбрана из гетероциклической группы, содержащей один или несколько гетероатомов, выбранных из О, S и N;
Alk2 обозначает необязательно замещенный низший алкил;
p равно 1 или 2;
если присутствует несколько W1, несколько W3 и несколько R12, каждый из них может иметь значение, независимо отличающееся от других;
его фармацевтически приемлемая соль или сольват.13. The compound according to any one of paragraphs.5-7, where cycle a has the formula
chemical formula 8
Figure 00000355
or
Figure 00000356

where R 9 , R 10 and R 11 represent a hydrogen atom: halogen, hydroxy, cyano, optionally substituted lower alkyl, optionally substituted lower alkoxy, optionally substituted lower alkenyl, optionally substituted lower alkynyl, carboxy, optionally substituted lower alkoxycarbonyl, optionally substituted amino, optionally substituted carbamoyl, optionally substituted lower alkylsulfonyl, optionally substituted carbocyclic group, or optionally substituted heterocyclic oxy group; and
G are a compound of the formula:
chemical formula 9
Figure 00000357
,
Figure 00000358
,
Figure 00000359
,
Figure 00000360
,
Figure 00000361
,
Figure 00000362
,
Figure 00000363
,
Figure 00000364
,
Figure 00000365
,
Figure 00000366
,
Figure 00000367
,
Figure 00000368
,
Figure 00000369
,
Figure 00000370
,
Figure 00000371

Figure 00000372
,
Figure 00000373
or
Figure 00000374

each of Q 1 , Q 2 and Q 3 independently represents a bond, an optionally substituted lower alkylene or an optionally substituted lower alkenylene;
Q 4 is optionally substituted lower alkylene or optionally substituted lower alkenylene;
each of W 1 and W 2 independently represents O or S;
W 3 is O, S or NR 12 ;
R 12 represents a hydrogen atom, lower alkyl, hydroxy lower alkyl, lower alkoxy lower alkyl, lower alkoxycarbonyl lower alkyl;
R 14 represents a hydrogen atom or lower alkyl;
cycle B is an optionally substituted carbocyclic group, where the carbocyclic group is optionally selected from an aryl and non-aromatic fused carbocyclic group, or an optionally substituted heterocyclic group, where the heterocyclic group is selected from a heterocyclic group selected from one, several heteroatoms selected from O, S and N;
Alk 2 is optionally substituted lower alkyl;
p is 1 or 2;
if several W 1 , several W 3 and several R 12 are present, each of them may have a value that is independently different from the others;
a pharmaceutically acceptable salt or solvate thereof. 14. Соединение по п.13, где цикл В представляет собой арил, необязательно замещенный одним или несколькими заместителями, выбранными из группы, включающей в себя галоген, гидрокси, необязательно замещенный низший алкил, необязательно замещенный низший алкокси, необязательно замещенный ацил, необязательно замещенный амино, циано, необязательно замещенный карбамоил, необязательно замещенную карбоциклическую группу, необязательно замещенную карбоциклическую оксигруппу и необязательно замещенную гетероциклическую группу, или
гетероарил, необязательно замещенный одним или несколькими заместителями, выбранными из группы, включающей в себя галоген, гидрокси, необязательно замещенный низший алкил, необязательно замещенный низший алкокси, необязательно замещенный ацил, необязательно замещенный амино, циано, необязательно замещенный карбамоил, необязательно замещенную карбоциклическую группу, необязательно замещенную карбоциклическую оксигруппу и необязательно замещенную гетероциклическую группу,
его фармацевтически приемлемая соль или сольват.14. The compound of claim 13, wherein cycle B is aryl optionally substituted with one or more substituents selected from the group consisting of halogen, hydroxy, optionally substituted lower alkyl, optionally substituted lower alkoxy, optionally substituted acyl, optionally substituted amino , cyano, optionally substituted carbamoyl, optionally substituted carbocyclic group, optionally substituted carbocyclic oxy group and optionally substituted heterocyclic group, or
heteroaryl optionally substituted by one or more substituents selected from the group consisting of halogen, hydroxy, optionally substituted lower alkyl, optionally substituted lower alkoxy, optionally substituted acyl, optionally substituted amino, cyano, optionally substituted carbamoyl, optionally substituted carbocyclic group, optionally a substituted carbocyclic oxy group and an optionally substituted heterocyclic group,
a pharmaceutically acceptable salt or solvate thereof. 15. Соединение по п.13, где G имеет формулу:
химическая формула 10
Figure 00000375
,
Figure 00000376
,
Figure 00000377
,
Figure 00000378
или
Figure 00000379
,
его фармацевтически приемлемая соль или сольват.15. The compound according to item 13, where G has the formula:
chemical formula 10
Figure 00000375
,
Figure 00000376
,
Figure 00000377
,
Figure 00000378
or
Figure 00000379
,
a pharmaceutically acceptable salt or solvate thereof. 16. Соединение по любому из пп.5-15, где R5 обозначает С1-С3 алкил, его фармацевтически приемлемая соль или сольват.16. The compound according to any one of claims 5-15, wherein R 5 is C1-C3 alkyl, a pharmaceutically acceptable salt or solvate thereof. 17. Соединение по любому из пп.5-7, где R5 обозначает метил, его фармацевтически приемлемая соль или сольват.17. The compound according to any one of claims 5 to 7, wherein R 5 is methyl, a pharmaceutically acceptable salt or solvate thereof. 18. Соединение по любому из пп.5-7, где каждый из R3a и R3b независимо обозначает атом водорода, необязательно замещенный низший алкил или необязательно замещенный арил, его фармацевтически приемлемая соль или сольват.18. The compound according to any one of claims 5 to 7, where each of R 3a and R 3b independently represents a hydrogen atom, optionally substituted lower alkyl or optionally substituted aryl, a pharmaceutically acceptable salt or solvate thereof. 19. Соединение по любому из пп.5-7, где все заместители R3a и R3b обозначают атом водорода, его фармацевтически приемлемая соль или сольват.19. The compound according to any one of claims 5 to 7, where all the substituents R 3a and R 3b represent a hydrogen atom, a pharmaceutically acceptable salt or solvate thereof. 20. Фармацевтическая композиция, обладающая ингибиторной активностью в отношении ВАСЕ 1, содержащая соединение по любому из пп.5-19, его фармацевтически приемлемую соль или сольват.20. A pharmaceutical composition having inhibitory activity against BACE 1, comprising a compound according to any one of claims 5-19, a pharmaceutically acceptable salt or solvate thereof. 21. Композиция с ингибиторной активностью в отношении ВАСЕ 1, содержащая соединение по любому из пп.5-19,
его фармацевтически приемлемую соль или сольват. 21. A composition with inhibitory activity against BACE 1 containing the compound according to any one of claims 5-19,
a pharmaceutically acceptable salt or solvate thereof.
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